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Федеральное государственное бюджетное учреждение науки
Новосибирский институт органической химии им. Н.Н. Ворожцова
Сибирского отделения Российской академии наук

Сотрудник:  Павлова Алла Викторовна
Занимаемые должности:  нс(кбн) ЛФИ


 

Публикации (по IF ) сотрудника подразделения БД НИОХ СО РАН

  1. O.V. Ardashov, A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, E.V. Karpova, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Highly potent activity of (1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol in animal models of Parkinson's disease
    J. Med. Chem., 2011, V. 54, N 11, 3866-74. doi:10.1021/jm2001579, IF=5.206
     
  2. O.V. Ardashov, A.V. Pavlova, A.K. Mahato, Yu. Sidorova, E.A. Morozova, D.V. Korchagina, G.E. Salnikov, A.M. Genaev, O.S. Patrusheva, N. Li-Zhulanov, T.G. Tolstikova, K.P. Volcho, N. Salakhutdinov
    A novel small molecule supports the survival of cultured dopamine neurons and may restore the dopaminergic innervation of the brain in the MPTP mouse model of Parkinson's disease
    ACS Chemical Neuroscience, Just Accepted Publication Date (Web):August 29, 2019 doi:10.1021/acschemneuro.9b00396, IF=3.861
     
  3. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    Antiparkinsonian activity of some 9-N-, O-, S- and C-derivatives of 3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol
    Bioorganic & Medicinal Chemistry, 2013, V. 21, N 5, P. 1082-1087. doi:10.1016/j.bmc.2013.01.003, IF=2.903
     
  4. K. Ponomarev, E. Morozova, A. Pavlova, E. Suslov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and Analgesic Activity of Amines Combining Diazaadamantane and Monoterpene Fragments
    Medicinal Chemistry, 2017, V. 13 , N 8, Pp 773 - 779 doi:10.2174/1573406413666170525124316, IF=2.331
     
  5. O. Mikhalchenko, I. Il’ina, A. Pavlova, E. Morozova, D. Korchagina, T. Tolstikova, E. Pokushalov, K. Volcho, N.Salakhutdinov
    Synthesis and analgesic activity of new heterocyclic compounds derived from monoterpenoids
    Medicinal Chemistry Research, 2013, V. 22, N 6, P. 3026-3034. doi:10.1007/s00044-012-0310-9, IF=1.611
     
  6. A. Sokolova, A. Pavlova, N. Komarova, O. Ardashov, A. Shernyukov, Yu. Gatilov, O. Yarovaya, T. Tolstikova, N. Salakhutdinov
    Synthesis and analgesic activity of new α-truxillic acid derivatives with monoterpenoid fragments
    Medicinal Chemistry Research, 2016, V. 25, N 8, pp 1608-1615 doi:10.1007/s00044-016-1593-z, IF=1.435
     
  7. I. Il’ina, O. Mikhalchenko, A. Pavlova, D. Korchagina, T. Tolstikova, K. Volcho, N. Salakhutdinov, E. Pokushalov
    Highly potent analgesic activity of monoterpene-derived (2S,4aR,8R,8aR)-2-aryl-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
    Medicinal Chemistry Research, 2014, V. 23, N 12, pp 5063-5073 doi:10.1007/s00044-014-1071-4, IF=1.402
     
  8. K. Ponomarev, A. Pavlova, E. Suslov, O. Ardashov, D. Korchagina, A. Nefedov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of new compounds combining azaadamantane and monoterpene moieties
    Medicinal Chemistry Research, 2015, V. 24, N 12, pp 4146-4156 doi:10.1007/s00044-015-1464-z, IF=1.401
     
  9. A. Pavlova, O. Mikhalchenko, A. Rogachev, I. Il'ina, D. Korchagina, Yu. Gatilov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of stereoisomers of 2-(3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8a-hexahydro-2H-chromene-4,8-diols
    Medicinal Chemistry Research, 2015, V 24, N 11, pp 3821-3830 doi:10.1007/s00044-015-1426-5, IF=1.401
     
  10. O.V. Ardashov, A.V. Pavlova, D.V. Korchagina, K.P. Volcho, T.G. Tolstikova, N.F. Salakhutdinov
    3-Methyl-6-(prop-1-en-2-yl) cyclohex-3-ene-1,2-diol: the Importance of Functional Groups for Antiparkinsonian Activity
    Medicinal Chemistry, 2013, V. 9, N 5, P. 731-739. doi:10.2174/1573406411309050013, IF=1.373
     
  11. I. Il'ina, A. Pavlova, D. Korchagina, O. Ardashov, T. Tolstikova, K. Volcho, N. Salakhutdinov
    Synthesis and analgesic activity of monoterpenoid-derived alkyl-substituted chiral hexahydro-2H-chromenes
    Medicinal Chemistry Research, 2017, V. 26, N 7, pp 1415-1426 doi:10.1007/s00044-017-1847-4, IF=1.276
     
  12. A. Pavlova, O. Patrusheva, I. Il'ina, K. Volcho, T. Tolstikova, N. Salakhutdinov
    The Decisive Role of Mutual Arrangement of Hydroxy and Methoxy Groups in (3(4)-hydroxy-4(3)-methoxyphenyl)-4,7-dimethyl-3,4,4a,5,8,8ahexahydro- 2H-chromene-4,8-diols in their Biological Activity
    Letters in Drug Design & Discovery, 2017, V. 14, N 5, pp. 508-514 doi:10.2174/1570180813666161102142642, IF=1.169
     
  13. A.V. Pavlova, I.V. Il'ina, E.A. Morozova, D.V. Korchagina, S.Yu. Kurbakova, I.V. Sorokina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Potent Neuroprotective Activity of Monoterpene Derived 4-[(3aR,7aS)-1,3,3a,4,5,7a-Hexahydro-3,3,6-trimethylisobenzofuran-1-yl]-2-methoxyphenol in MPTP Mice Model
    Letters in Drug Design & Discovery, 2014, V. 11 N 5 pp. 611-617. doi:10.2174/1570180811666131210000316, IF=0.961
     
  14. T.G. Tolstikova, A.V. Pavlova, E.A. Morozova, T.M. Khomenko, K.P. Volcho, N.F. Salakhutdinov
    The analgesic activity of 8- ( trifluoromethyl)-1,2,3,4,5-benzopentathiepine-6-amine and its hydrochloride
    Lett. Drug Des. Discov., 2012, V. 9, N 5, 513-516. doi:10.2174/157018012800389296, IF=0.871
     
  15. A.V. Pavlova, E.V. Nazimova, O.S. Mikhal'chenko, I.V. Il'ina, D.V. Korchagina, O.V. Ardashov, E.A. Morozova, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2H-Chromen-4,8-Diols Containing Thiophene Substituents
    Chemistry of Natural Compounds, , 2016, V. 52, N 5, pp 813-820 doi:10.1007/s10600-016-1785-2, IF=0.472
     
  16. O.S. Patrusheva, A.V. Pavlova, D.V. Korchagina, T.G. Tolstikova, K.P. Volcho, N.F. Salakhutdinov
    Synthesis and Analgesic Activity of 4,7-Dimethyl-3,4,4a,5,8,8a-Hexahydro-2-Chromen-4,8-Diols Containing Alkyl-Substituted Aromatic Moieties
    Chemistry of Natural Compounds, 2017, V. 53, N 6, Pp 1066-1071 doi:10.1007/s10600-017-2202-1, IF=0.46
     
  17. Т.Г. Толстикова, Е.А. Морозова, А.В. Павлова, А.В. Болкунов, М.П. Долгих, Е.А. Конева, К.П. Волчо, Н.Ф. Салахутдинов, Г.А. Толстиков
    Производные аминокислот пинанового ряда – новые противосудорожные агенты.
    Доклады АН, 2008, Т. 422, № 4, 490-492. (Derivatives of Pinane Amino Acids as New Anticonvulsants/ T. G. Tolstikova, E. A. Morozova, A. V. Pavlova, A. V. Bolkunov, M. P. Dolgikh, E. A. Koneva, K. P. Volcho, N. F. Salakhutdinov, G. A. Tolstikov// Doklady Chemistry, 2008, V. 422, N 2, pp 248-250 doi:10.1134/S0012500808100029), IF=0.442
     
  18. А.В. Душкин, Е.С. Метелева, Т.Г. Толстикова, А.В. Павлова, М.В. Хвостов
    Гель-хроматографическое и токсикологическое исследование механохимических превращений водорастворимых полисахаридов
    Хим.-фарм. журн., 2012, Т. 46, № 10, 53-56. (Gel chromatographic and toxicological studies of the mechanochemical transformations of water-soluble polysaccharides/ A. V. Dushkin, E. S. Meteleva, T. G. Tolstikova, A. V. Pavlova, M. V. Khvostov// PHARM CHEM J+, 2012, V. 46, N 10, pp. 630-633. doi:10.1007/s11094-013-0859-8), IF=0.372
     


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